Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Restaurant Eating...is It A Possibility?


jewlr22

Recommended Posts

jewlr22 Newbie

Hello out there....

I am recently diagnosed with celiac through the blood tests...I have not been "scoped", or biopsied yet due to the fact that I have medicaid and it is very difficult to find a Dr. that will perform the procedure. I guess they don't pay enough.....Anyway...I am trying like heck to eat right, but I feel like such a downer on my family-we used to eat out all the time, not just junk food, but real food too, and now everything has changed....I am wondering first of all if there are any reccommendations anyone has to how you eat out or where to eat out and I am also wondering about putting the whole family (2- 10 year old sons and a wonderful dad ) on a gluten free diet. I am just concerned about their tastes---any suggestions there too??

I am starting to go into the depression I have heard goes along with such a drastic change in life, and really could use some support.

Thank you for listening........


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



bscarter46 Newbie

Hi jewlr22. I am not yet diagnosed but my doctor thinks I may also have celiac disease. I had both antibodies come back positive but the endomysial was negative. I'm still waiting on a call back from my doctor to see what this means. I have been reading a lot on this and I think there is a board about eating out and also you can go to the restaraunts websites and some have gluten-free menu's. The places so far that I have found with online gluten-free menu's are Wendy's, McDonalds, Outback Steakhouse, Chili's, Chik-fil-A, Steak N Shake and Burger King(has I think items containing wheat on their nutrition menu, not an actual gluten-free menu). If I do go on the diet my husband already says he will go on it with me. I think someone mentioned it is healthier than any diet. I am currently in a depression because it has been two years and even though I feel closer to finding out what is wrong with me, I also feel like we will never find out. I guess with the high antibody levels that I at least have a gluten intolerance, if not celiac. I hate the thought of going on the diet, but at least it is an answer and will get easier with time. Good luck and even though I don't know much, I hope I helped you some! Take care!

Guest jhmom

HI, if you have been dx through blood-work then there is really no reason to be scoped, you should be adhereing to a strict gluten free diet for life. For me I only eat at restaurants that offer a gluten-free menu because you never know what kind of spices are used or if they marinate their meats.

Here on the board there is a section "gluten-free dining and eating out", there are a lot of posts about certain restaurants that serve gluten-free meals and also posts in certain States.....

Here are some websites where you can look at gluten-free menus

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Open Original Shared Link

Also I have heard PH Changs has a gluten-free menu

Guest gillian502

I wouldn't suggest eating out until all your symptoms have vastly improved and your antibodies have become normal. This will probably take 6 to 12 months, but I feel it's worth it. The less suspicious foods you eat, the faster you will heal. I've read that a lot of people here are comfortable eating at places like Wendy's and McDonalds...personally I wouldn't touch those places with a ten foot pole. I don't believe for one second that places like that are careful with cross-contamination issues; for goodness sake, there's teenagers running them! I would also say get the biopsy, just to confirm your diagnosis so you won't be fending off the drs. all your life telling you to just get one already, because they will do that.

hapi2bgf Contributor

I used to eat out a couple of times a week before celiacs and now I do not eat out as much - but I do go. For me and the people I know, eating out is as much a social activity as it is just getting a meal. In my own opinion, I will not let this diet force me to never eat out again. On that same note, I am very careful about where I go and what I eat, and when I go on trips I pack A LOT of gluten-free foods. But everyone has to make the decision about how to make this diet work for them and their life style.

Here's what I did when I was diagnosed. Maybe some of it will appeal to you.

1. Learn as much about the diet as you can and be able to explain it to someone who has no idea such a crazy disease ever existed. Be able to laugh about the disease - it puts the other people at ease.

2. Call you favorite restaurants between 2 and 4pm when they are slower and ask to speak with a manager. Ask if they have time now to talk to you about food allergies. Explain that you used to eat there regularly and your family really enjoys the food. You are trying to find one or two menu items that you can eat. Ask for plain non-marinaded meat with no seasonings, etc. Generally the managers have been extremely helpful to me. I have had managers pass me off to the regonal manager when they did not know the answers. And I have managers stand in the fridge and read lables.

3. Realize that eating out will be a bit boring compared to what you used to eat.

4. If in doubt of a restaurants ability to handle your diet (when you have no choice in where you are eating) bring a hot baked potato, cooked meat to add to a plain salad, and any dressing or condiments you might need. I stuff quite a bit in the diaper bag :P

Another concern is figuring out which family and friends want to learn how to cook something gluten-free and which ones just have no intention of dealing with it. To date, my friends are doing great cooking gluten-free and my family has no intention of dealing with it. So be it. I eat first or bring my own food to family events and make myself at home in their kitchen.

Best of luck!

  • 2 months later...
snoopini Newbie

Although there are places that have gluten-free menus, please be aware that they DO NOT always practice safe food handling. Subway for example does not wash their knifes after cutting rolls, plus the amount of crumbs around that place make me gag!! I frequent my local Outback BUT that was only after writing a very nasty letter to Outback after receiving croutons in my salad , or finding crumbs at the bottom of the bowl after eating my salad - SIX times this happened to me. I have spoken to the proprietor and he now knows that the food must be handled separately. Most people think that if we eat a little bit of gluten that's it's like being lactose intolerant. People think that you will have an upset stomach and that's it's not a big deal. Remember that ignorance is bliss, we are the ones who will be sick for a week, not them, they have no idea what it's like. I was also told by one of my local italian restaurants that I could bring my own pasta and eat their sauce, BUT after further investigation, I found out they use broth in their sauce which the chef had no idea had gluten in it. It's hard to eat out. I go to my local Wendys alot because their chili is supposed to be gluten free but if I go to the Wendys by my work I get sick...it's sad how many foods are gluten free but the handling of the food makes you sick. Just make sure the people know that nothing can touch the food as well, rinsing utensils isn't enough. I still have to remind my family of this as well!! Good luck! I'm sick today for some unknown reason....and my whole house is gluten-free!!

dkmb Newbie

With eating out you need to be pro-active and let the place you plan to eat at know your concerns. There are many posts as mentioned, on here about calling ahead, talking to the chef, and some people carry cards that tell about celiac disease.

My granddaugther just had a wonderful experience at the Jungle (like Chuckie Cheese). Her aunt called ahead and they said she could bring her own food. They brought a pizza with them on aluminum foil. The Jungle heated it up for her with a note that it was not to touch any other food in big letters!

It really can be a very healthy diet with the concentration more on fresh foods of all kinds, since you don't have to worry about hidden gluten. :D

DK


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to McKinleyWY's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Accuracy of testing concerns

    2. - McKinleyWY posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Accuracy of testing concerns

    3. - trents replied to Teaganwhowantsanexpltion's topic in Introduce Yourself / Share Stuff
      4

      A little about me and my celiac disease

    4. - Peace lily replied to AristotlesCat's topic in Super Sensitive People
      118

      Gluten Free Coffee

    5. - Teaganwhowantsanexpltion replied to Teaganwhowantsanexpltion's topic in Introduce Yourself / Share Stuff
      4

      A little about me and my celiac disease

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,238
    • Most Online (within 30 mins)
      7,748

    tcpb
    Newest Member
    tcpb
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Welcome to the celiac.com community, @McKinleyWY! There currently is no testing for celiac disease that does not require you to have been consuming generous amounts of gluten (at least 10g daily, about the amount in 4-6 slices of wheat bread) for at least two weeks and, to be certain of accurate testing, longer than that. This applies to both phases of testing, the blood antibody tests and the endoscopy with biopsy.  There is the option of genetic testing to see if you have one or both of the two genes known to provide the potential to develop celiac disease. It is not really a diagnostic measure, however, as 30-40% of the general population has one or both of these genes whereas only about 1% of the general population actually develops celiac disease. But genetic testing is valuable as a rule out measure. If you don't have either of the genes, it is highly unlikely that you can have celiac disease. Having said all that, even if you don't have celiac disease you can have NCGS (Non Celiac Gluten Sensitivity) which shares many of the same symptoms as celiac disease but does not involve and autoimmune reaction that damages the lining of the small bowel as does celiac disease. Both conditions call for the complete elimination of gluten from the diet. I hope this brings some clarity to your questions.
    • McKinleyWY
      Hello all, I was diagnosed at the age of 2 as being allergic to yeast.  All my life I have avoided bread and most products containing enriched flour as they  contain yeast (when making the man made vitamins to add back in to the flour).  Within the last year or so, we discovered that even whole wheat products bother me but strangely enough I can eat gluten free bread with yeast and have no reactions.  Obviously, we have come to believe the issue is gluten not yeast.  Times continues to reinforce this as we are transitioning to a gluten free home and family.  I become quite ill when I consume even the smallest amount of gluten. How will my not having consumed breads/yeast/gluten for the better part of decades impact a biopsy or blood work?  I would love to know if it is a gluten intolerance or a genetic issue for family members but unsure of the results given my history of limited gluten intake.   I appreciate the input from those who have gone before me in experience and knowledge. Thank you all!
    • trents
      I know what you mean. When I get glutened I have severe gut cramps and throw up for 2-3 hr. and then have diarrhea for another several hours. Avoid eating out if at all possible. It is the number one source of gluten contamination for us celiacs. When you are forced to eat out at a new restaurant that you are not sure is safe, try to order things that you can be sure will not get cross contaminated like a boiled egg, baked potatos, steamed vegies, fresh fruit. Yes, I know that doesn't sound as appetizing as pizza or a burger and fries but your health is at stake. I also realize that as a 14 year old you don't have a lot of control over where you eat out because you are tagging along with others or adults are paying for it. Do you have support from your parents concerning your need to eat gluten free? Do you believe they have a good understanding of the many places gluten can show up in the food supply?
    • Peace lily
      Okay went online to check green mountain k cups .It was said that the regular coffees are fine but they couldn’t guarantee cross contamination.with the flavors. im trying to figure out since I eliminated the suyrup so far so good. I’m hoping. thanks it feels good to listen to other people there views.
    • Teaganwhowantsanexpltion
      Thank you I will i have been on a strict gluten free diet ever since I got diagnosed but sometimes places lie about there food so there r some things that do get contaminated which causes me to throw up on end for several hours until I can't hold myself up anymore 
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.